Sr. Engineering Validation Associate
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Job Location:
Sanford, FL - USA
Monthly Salary:
$ 80300 - 133900
Posted on:
15-10-2025
Vacancies:
1 Vacancy
Job Summary
Use Your Power for Purpose
Every day our unwavering commitment to quality ensures the delivery of safe and effective products to patients. Our innovative flexible and customer-oriented culture is rooted in science and risk-based compliance. Whether you are engaged in development maintenance compliance or research analysis your contributions have a direct impact on patient care.
What You Will Achieve
In this role you will:
Execute work independently work with various groups across the organization and be able to oversee and lead projects to ensure cGMP automated systems perform as intended.
Evaluate review and approve validation master plans protocols and reports ensuring compliance with company standards and regulatory requirements.
Troubleshoot validation issues for equipment and performance processes providing expertise for resolution.
Provide commissioning qualification and verification support for all cGMP automated systems at the Sanford site related to the manufacture of biological drug substances and drug substances intermediates.
Contribute to moderately complex projects manage time effectively and develop plans for short-term work activities.
Manage routine Quality systems such as Change Control Quality Agreement Documentation and Investigations and coordinate testing with functional groups.
Maintain the Site Validation Master Plan support regulatory audits and represent engineering validation on site or network teams.
Support product transfers new product development regulatory queries cost improvement projects and Cleaning Validation ensuring integration of validation schedules in production and participating in deviation investigations.
Here Is What You Need (Minimum Requirements)
Applicant must have a bachelors degree with at least 2 years of experience; OR a masters degree with 0 years of experience;
OR an associates degree with 6 years of experience; OR a high school diploma (or equivalent) and 8 years of relevant experienceProven expertise in Good Manufacturing Practices
Strong working knowledge of various quality systems and processes
Familiarity with information systems such as Global Document Management System System Application & Products and Quality Tracking System
Excellent verbal and written communication skills
Ability to work independently and in a team environment
Bonus Points If You Have (Preferred Requirements)
Strong technical knowledge with validation/qualification of pharmaceutical processes equipment utilities facilities and/or computer systems
Experience with sterile products and medical devices
Strong analytical and problem-solving skills
Strong organizational and time management skills
Ability to mentor and guide other colleagues
Experience in regulatory audits and compliance
OTHER JOB DETAILS
Last Date to Apply for Job: October 23 2025.
Referral Bonus Eligibility: YES
Eligible for Relocation Package: NO
Work Location Assignment:On Premise
Relocation assistance may be available based on business needs and/or eligibility.
Sunshine Act
Pfizer reports payments and other transfers of value to health care providers as required by federal and state transparency laws and implementing regulations. These laws and regulations require Pfizer to provide government agencies with information such as a health care providers name address and the type of payments or other value received generally for public disclosure. Subject to further legal review and statutory or regulatory clarification which Pfizer intends to pursue reimbursement of recruiting expenses for licensed physicians may constitute a reportable transfer of value under the federal transparency law commonly known as the Sunshine Act. Therefore if you are a licensed physician who incurs recruiting expenses as a result of interviewing with Pfizer that we pay or reimburse your name address and the amount of payments made currently will be reported to the government. If you have questions regarding this matter please do not hesitate to contact your Talent Acquisition representative.
EEO & Employment Eligibility
Pfizer is committed to equal opportunity in the terms and conditions of employment for all employees and job applicants without regard to race color religion sex sexual orientation age gender identity or gender expression national origin disability or veteran status. Pfizer also complies with all applicable national state and local laws governing nondiscrimination in employment as well as work authorization and employment eligibility verification requirements of the Immigration and Nationality Act and IRCA. Pfizer is an E-Verify employer. This position requires permanent work authorization in the United States.
Pfizer endeavors to make to all users. If you would like to contact us regarding the accessibility of our website or need assistance completing the application process and/or interviewing please email. This is to be used solely for accommodation requests with respect to the accessibility of our website online application process and/or interviewing. Requests for any other reason will not be returned.
Required Experience:
Senior IC
Key Skills
- Python
- SOC
- Debugging
- C/C++
- FDA Regulations
- Minitab
- Technical Writing
- GAMP
- OS Kernels
- Perl
- cGMP
- Manufacturing
About Company
Erfahren Sie mehr über uns als forschendes und produzierendes Pharmaunternehmen: Von unserem Beitrag zum medizinischen Fortschritt bis zur nachhaltigen Produktion.
